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叶酸/维生素 B 可减轻高同型半胱氨酸血症诱导的大鼠视网膜阿尔茨海默病样病变。

Folate/Vitamin B Alleviates Hyperhomocysteinemia-Induced Alzheimer-Like Pathologies in Rat Retina.

机构信息

Department of Pathophysiology, School of Basic Medicine and Collaborative Innovation Center for Brain Science, Key Laboratory for Neurological Disorders of the Ministry of Education of China, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.

Emergency Department, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.

出版信息

Neurosci Bull. 2019 Apr;35(2):325-335. doi: 10.1007/s12264-018-0293-8. Epub 2018 Sep 28.

Abstract

Hyperhomocysteinemia (Hhcy) is an independent risk factor for Alzheimer's disease (AD). Visual dysfunction is commonly found and is positively correlated with the severity of cognitive defects in AD patients. Our previous study demonstrated that Hhcy induces memory deficits with AD-like tau and amyloid-β (Aβ) pathologies in the hippocampus, and supplementation with folate and vitamin B12 (FB) prevents the Hhcy-induced AD-like pathologies in the hippocampus. Here, we investigated whether Hhcy also induces AD-like pathologies in the retina and the effects of FB. An Hhcy rat model was produced by vena caudalis injection of homocysteine for 14 days, and the effects of FB were assessed by simultaneous supplementation with FB in drinking water. We found that Hhcy induced vessel damage with Aβ and tau pathologies in the retina, while simultaneous supplementation with FB remarkably attenuated the Hhcy-induced tau hyperphosphorylation at multiple AD-related sites and Aβ accumulation in the retina. The mechanisms involved downregulation of amyloid precursor protein (APP), presenilin-1, beta-site APP-cleaving enzyme 1, and protein phosphatase-2A. Our data suggest that the retina may serve as a window for evaluating the effects of FB on hyperhomocysteinemia-induced Alzheimer-like pathologies.

摘要

高同型半胱氨酸血症(HHcy)是阿尔茨海默病(AD)的独立危险因素。视觉功能障碍在 AD 患者中很常见,且与认知缺陷的严重程度呈正相关。我们之前的研究表明,HHcy 可导致海马中出现 AD 样 tau 和淀粉样β(Aβ)病理学,并可通过补充叶酸和维生素 B12(FB)预防 HHcy 诱导的海马 AD 样病理学。在这里,我们研究了 HHcy 是否也会在视网膜中诱导 AD 样病理学以及 FB 的作用。通过尾静脉注射同型半胱氨酸 14 天来制备 HHcy 大鼠模型,并通过同时在饮水中补充 FB 来评估 FB 的作用。我们发现 HHcy 可诱导视网膜血管损伤和 Aβ及 tau 病理学,而同时补充 FB 可显著减轻 HHcy 诱导的视网膜中多个 AD 相关位点的 tau 过度磷酸化和 Aβ积累。其机制涉及下调淀粉样前体蛋白(APP)、早老素-1、β位 APP 裂解酶 1 和蛋白磷酸酶-2A。我们的数据表明,视网膜可能作为评估 FB 对 HHcy 诱导的 AD 样病理学作用的窗口。

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